Evidence map›Paper›PMID 32533504›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2020

Metabolomic study of disease progression in scrapie prion infected mice; validation of a novel method for brain metabolite extraction.

Ze-Lin Fu, Pascal Mercier, Ghazaleh Eskandari-Sedighi, Jing Yang, David Westaway, Brian D Sykes

Abstract read
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In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 50% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Quaternary Structure Changes for PrPMolecular neurobiology · 2021
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Ze-Lin FuDepartment of Biochemistry, University of Alberta, Edmonton, AB, Canada.
Pascal MercierNational High Field Nuclear Magnetic Resonance Centre (NANUC), Edmonton, AB, Canada.
Ghazaleh Eskandari-SedighiDepartment of Biochemistry, University of Alberta, Edmonton, AB, Canada.
Jing YangCentre for Prions and Protein Folding Diseases, University of Alberta, Edmonton, AB, Canada.
David WestawayDepartment of Biochemistry, University of Alberta, Edmonton, AB, Canada.
Brian D SykesDepartment of Biochemistry, University of Alberta, Edmonton, AB, Canada. brian.sykes@ualberta.ca.ORCID 0000-0003-2544-2246
University of Alberta · CA

Funding

CIHR MOP137094
6 · The paper itself

Abstract

introductionPrion disease is a form of neurodegenerative disease caused by the misfolding and aggregation of cellular prion protein (PrP

objectivesThe intention was to identify and quantify the small-in-size and water-soluble metabolites extracted from mice brains infected with the Rocky Mountain Laboratory isolate of mouse-adapted scrapie prions (RML) and track changes in these metabolites during disease evolution.

methodsA total of 73 mice were inoculated with RML prions or normal brain homogenate control; brains were harvested at 30, 60, 90, 120 and 150 days post-inoculation (dpi). We devised a high-efficiency metabolite extraction method and used nuclear magnetic resonance spectroscopy to identify and quantify 50 metabolites in the brain extracts. Data were analyzed using multivariate approach.

resultsBrain metabolome profiles of RML infected animals displayed continuous changes throughout the course of disease. Among the analyzed metabolites, the most noteworthy changes included increases in myo-inositol and glutamine as well as decreases in 4-aminobutyrate, acetate, aspartate and taurine.

conclusionWe report a novel metabolite extraction method for lipid-rich tissue. As all the major metabolites are identifiable and quantifiable by magnetic resonance spectroscopy, this study suggests that tracking of neurochemical profiles could be effective in monitoring the progression of neurodegenerative diseases and useful for assessing the efficacy of candidate therapeutics.

Indexed as

AnimalsBrainDisease ProgressionFemaleMaleMetabolomeMetabolomicsMiceMice, Inbred StrainsNeurodegenerative DiseasesPrionsScrapiePrionsMetabolomicsMultivariate approach nuclear magnetic resonance spectroscopyPrion disease

Identifiers

PMID32533504
OpenAlexW3034608573

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.